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Ground Glass Lesions
• Fibrous Dysplasia• Chronic Sclerosing
Osteomyelitis• Osteitis Deformans (early
phases)• Hyperparathyroidism• Osteopetrosis
Fibrous Dysplasia
• Childhood Onset• Growth cessation at Puberty• Expansile, Nondemarcated• Bone panel is normal• Cosmetic Osseous Contouring• Monostotic or Polyostotic
Fibrous Dysplasia
• Monostotic• Polyostotic• McCune-Albright
– Polyostotic– Endocrinopathies– Café au Lait Pigmentation– Mutation with Lyonization
Chronic Sclerosing Osteomyelitis
• Childhood onset• Bacterial infection
– anaerobic• ? Source – odontogenic• Poorly marginated• Episodic Pain• Culture/Sensitivity
Osteitis Deformans (Paget’s)
• Elderly• Polyostotic Lesions• Progressive Opacification• Cranial Nerve Deficits• Alkaline Phosphatase• Normal Calcium• Giant Cell Tumors• Sarcomas
Hyperparathyroidism
• Primary Parathyroid Adenoma• Secondary to Renal Disease• Diffuse, Poorly Marginated• Loss of Lamina Dura• Hypercalcemia, Calciuria• Brown Tumors• Urolithiasis
Osteopetrosis (Marble Bone)Albers-Shonberg Disease
A diverse group of diseases genotypically with a commonPhenotype
Defective osteoclastic resorption
Inherited as automsomal dominant or recessive
Mutations in Carbonic anhydrase II, subunit of vacuolar protein pump of the brush border, cathepsin K (Pycnodysostosis)
Diffuse ground glass opacification that may obscure theImage of teeth radiographically
Myelophthisic anemia with thrombocytopenia